A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249185



Internal ID20816225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100227865..100228719hg38UCSC Ensembl
chr1:100693421..100694275hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551203
Supporting Variants
Samples
Known GenesDBT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249185
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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